Effectiveness and Safety of Immune Checkpoint Inhibitors in Cancer Patients With Autoimmune Disease: A Retrospective Cohort Study.


Journal

Journal of immunotherapy (Hagerstown, Md. : 1997)
ISSN: 1537-4513
Titre abrégé: J Immunother
Pays: United States
ID NLM: 9706083

Informations de publication

Date de publication:
06 Nov 2023
Historique:
received: 17 05 2023
accepted: 04 10 2023
medline: 8 11 2023
pubmed: 8 11 2023
entrez: 8 11 2023
Statut: aheadofprint

Résumé

Although immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment, patients with pre-existing autoimmune diseases (PADs) have largely been excluded from clinical trials evaluating this drug class. This study evaluates the effectiveness and safety of ICI therapy in individuals with PAD in a real-world setting. A retrospective study of patients exposed to ICI therapy between 2012 and 2019 was conducted. Patients with PAD were identified and matched to an ICI-exposed group without PAD based on age, sex, and cancer type. Primary outcomes included toxicity, time to treatment failure, overall survival, and objective response rate. The association between PAD status and outcomes was determined using Cox and logistic regression modeling. A total of 813 patients exposed to ICI therapy were identified, of which 8.2% (N=67) had a PAD. When compared with a matched cohort without PAD (N=132), there was no significant difference in the rates of new immune-related adverse events (irAEs, 42.4% in the non-PAD group vs. 47.8% in the PAD group, P=0.474). After controlling for the type of ICI, there was no significant association between PAD status and irAE (odds ratio 1.67, 95% CI: 0.9-3.21 P=0.1). There was no significant association between overall survival and PAD status (hazard ratio 1.12, 95% CI: 0.76-1.66. P=0.56) or between time to treatment failure and PAD status (hazard ratio 0.82, 95% CI: 0.6-1.12, P=0.22). There was an association between PAD status and objective response rate (odds ratio 3.28, 95% CI: 1.28-8.38, P=0.013). In summary, PAD status was not associated with enhanced toxicity when compared with patients without PAD, with similar oncologic effectiveness between these 2 groups.

Identifiants

pubmed: 37937529
doi: 10.1097/CJI.0000000000000492
pii: 00002371-990000000-00073
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Arjun A Raghavan (AA)

Rady Faculty of Health Sciences, University of Manitoba.

Sid Goutam (S)

Rady Faculty of Health Sciences, University of Manitoba.
Shared Health Manitoba.

Grace Musto (G)

CancerCare Manitoba, Winnipeg, MB.

Marc Geirnaert (M)

CancerCare Manitoba, Winnipeg, MB.

Carrie Ye (C)

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Liam J O'Neil (LJ)

Rady Faculty of Health Sciences, University of Manitoba.

Jeffrey Graham (J)

Rady Faculty of Health Sciences, University of Manitoba.
CancerCare Manitoba, Winnipeg, MB.

Classifications MeSH